Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region



Chrom. Start End TF Name Source Predicted site? Tissue/Cell line id More
chr8 13562840 13562845 USF2 TRANSFAC yes 68318607
chr8 13562851 13562855 H4TF2 TRANSFAC yes 68318608
chr8 13562851 13562870 CTCF JASPAR yes 68318609
chr8 13562854 13562873 CTCF JASPAR yes 68318610
chr8 13562859 13562870 E2F6 JASPAR yes 68318611
chr8 13562864 13562885 ZNF263 JASPAR yes 68318612
chr8 13562881 13562888 NFATC2 JASPAR yes 68318613
chr8 13562882 13562892 RELA JASPAR yes 68318614
chr8 13562900 13562910 SP1 JASPAR yes 68318615
chr8 13562911 13562915 H1TF2 TRANSFAC yes 68318616
chr8 13562911 13562915 NFE TRANSFAC yes 68318617
chr8 13562911 13562915 SRF TRANSFAC yes 68318618
chr8 13562919 13562929 TFAP4 JASPAR yes 68318619
chr8 13562966 13562981 PRDM1 JASPAR yes 68318620
chr8 13562984 13562997 TFAP2A JASPAR yes 68318621
chr8 13562984 13562997 TFAP2B JASPAR yes 68318622
chr8 13562992 13563012 TP63 JASPAR yes 68318623
chr8 13563006 13563017 FOXH1 JASPAR yes 68318624
chr8 13563016 13563026 MAX JASPAR yes 68318625
chr8 13563017 13563035 TP53 JASPAR yes 68318626
chr8 13563039 13563054 HNF4A JASPAR yes 68318627
chr8 13563040 13563054 NR2F1 JASPAR yes 68318628
chr8 13563040 13563055 HNF4G JASPAR yes 68318629
chr8 13563047 13563062 LEF1 JASPAR yes 68318630
chr8 13563048 13563062 TCF7L2 JASPAR yes 68318631
chr8 13563063 13563068 MYC TRANSFAC yes 68318632
chr8 13563099 13563102 MYB TRANSFAC yes 68318633
chr8 13563103 13563114 TBX20 JASPAR yes 68318634
chr8 13563130 13563146 SOX4 JASPAR yes 68318635
chr8 13563130 13563146 SOX8 JASPAR yes 68318636
chr8 13563138 13563150 HNF1B JASPAR yes 68318637
chr8 13563146 13563149 MYB TRANSFAC yes 68318638
chr8 13563159 13563166 SPIB JASPAR yes 68318639
chr8 13563166 13563176 SP1 JASPAR yes 68318640
chr8 13563177 13563181 H4TF2 TRANSFAC yes 68318641
chr8 13563198 13563203 SP1 TRANSFAC yes 68318642

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr8 13562835 rs114377668 T A no 10301122
chr8 13562861 rs79917126 G A
10301123
chr8 13562864 rs34734057 G T 10301124
chr8 13562887 rs35854225 A C,T
10301125
chr8 13562889 rs73221654 C G
10301126
chr8 13562907 rs74630908 G T
10301127
chr8 13562939 rs150480455 C T no 10301128
chr8 13562950 rs66960838 T C no 10301129
chr8 13562957 rs114764001 C T no 10301130
chr8 13562958 rs138331099 G A,T no 10301131
chr8 13562979 rs188083157 T A
10301132
chr8 13562990 rs149178479 C T 10301133
chr8 13562995 rs1481907 G C 10301134
chr8 13563020 rs143352361 T C
10301135
chr8 13563030 rs116049991 C G
10301136
chr8 13563102 rs71522377 A G
10301137
chr8 13563106 rs142435763 G A
10301138
chr8 13563158 rs7012989 C G no 10301139
chr8 13563163 rs77805882 C T
10301140
chr8 13563175 rs532418967 C G,T
10301141
chr8 13563181 rs547341218 CCAGGT C
10301142
chr8 13563188 rs566853615 T A no 10301143

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance between enhancer and TSS id More

No results

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand miRNA Name miRBase ID TSS Score TSI of Normal tissues TSI of Cancer tissues id More

No results